91735-33-0 Usage
Properties
1. Name: 2-[methyl(5H-purin-6-yl)amino]ethanol
2. Also known as: adenosine
3. Type: purine nucleoside
4. Natural component of RNA
5. Role: regulation of blood flow, neurotransmission, and immune response
6. Acts as a signaling molecule in the brain
7. Medicinal use: treatment of irregular heart rhythms
8. Diagnostic use: evaluation of heart function
9. Potential therapeutic applications in cancer and neurodegenerative diseases
Specific content
Plays crucial role in biochemical processes in the body
Involved in regulation of blood flow, neurotransmission, and immune response
Acts as a signaling molecule in the brain, modulating neuronal activity and promoting sleep and relaxation
Used as a medication to treat certain types of irregular heart rhythms
Used as a diagnostic tool to evaluate heart function
Studied for potential therapeutic applications in the treatment of cancer and neurodegenerative diseases
Check Digit Verification of cas no
The CAS Registry Mumber 91735-33-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,7,3 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 91735-33:
(7*9)+(6*1)+(5*7)+(4*3)+(3*5)+(2*3)+(1*3)=140
140 % 10 = 0
So 91735-33-0 is a valid CAS Registry Number.
91735-33-0Relevant articles and documents
A Study on the Intramolecular Mitsunobu Reaction of N6-(ω-Hydroxyalkyl)adenines
?im?nková, Nadě?da,Tobrman, Tomá?,Eigner, Václav,Dvo?ák, Dalimil
, p. 3565 - 3573 (2017/11/21)
The cyclization of N6-(ω-hydroxyalkyl)adenines with a N6H-group leads to N6,N1 ring closure regardless of the method of the cyclization that was used. Five-membered to eight-membered rings were obtained using NBS/PPh3; however, under Mitsunobu conditions, the eight-membered fused purine was not formed. Surprisingly, the cyclization of N6-methyl-N6-(4-hydroxybutyl)adenine only leads to N6,N7 ring closure using both methods.
